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在接受人生长激素治疗的克雅氏病患者中检测14-3-3蛋白脑脊液

14-3-3 protein cerebrospinal fluid detection in human growth hormone-treated Creutzfeldt-Jakob disease patients.

作者信息

Brandel J P, Peoc'h K, Beaudry P, Welaratne A, Bottos C, Agid Y, Laplanche J L

机构信息

Centre National de Référence de la MCJ iatrogène, H pital de la Salpêtrière, INSERM U360, Paris, France.

出版信息

Ann Neurol. 2001 Feb;49(2):257-60. doi: 10.1002/1531-8249(20010201)49:2<257::aid-ana48>3.0.co;2-x.

Abstract

The usefulness of the detection of 14-3-3 protein in the cerebrospinal fluid (CSF) in the diagnosis of Creutzfeldt-Jakob disease transmitted from human growth hormone was evaluated in 20 French patients. The 14-3-3 protein was rarely detectable within the first 3 months of the disease but always positive after 7 months associated with the aggravation of the disease and the occurrence of dementia. 14-3-3 detection was not predictive of the survival time of the patients. The genotype at PRNP codon 129 could influence the timing of appearance of the 14-3-3 protein in the CSF.

摘要

在20名法国患者中评估了检测脑脊液(CSF)中14-3-3蛋白在诊断由人生长激素传播的克雅氏病中的作用。在疾病的前3个月内很少能检测到14-3-3蛋白,但在7个月后总是呈阳性,这与疾病的加重和痴呆的发生有关。14-3-3检测不能预测患者的生存时间。PRNP密码子129处的基因型可能会影响CSF中14-3-3蛋白出现的时间。

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